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爱泼斯坦-巴尔病毒阳性T细胞和NK细胞淋巴增殖性疾病:2023年SH/EA4HP淋巴瘤研讨会报告

Epstein-Barr virus-positive T- and NK-cell lymphoproliferative disorders: Report from the 2023 SH/EA4HP Lymphoma Workshop.

作者信息

Quintanilla-Martinez Leticia, Li Shaoying, Chadburn Amy

机构信息

Institute of Pathology and Neuropathology, University Hospital Tuebingen and Comprehensive Cancer Center, Tuebingen, Germany.

Department of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, United States.

出版信息

Am J Clin Pathol. 2025 Jul 11;164(1):46-64. doi: 10.1093/ajcp/aqaf020.

DOI:10.1093/ajcp/aqaf020
PMID:40619129
Abstract

OBJECTIVES

To summarize the conclusions of the 2023 Society for Hematopathology/European Association for Haematopathology workshop regarding Epstein-Barr virus (EBV)-positive T- and natural killer (NK)-cell lymphoproliferative disorders (LPDs).

METHODS

There were 38 cases submitted to session 3 of the workshop.

RESULTS

Cases included extranodal NK/T-cell lymphoma (ENKTCL), nasal type (n = 16), EBV+ T- and NK-cell LPDs in children (n = 12), primary nodal EBV+ T- and NK-cell lymphoma (n = 5), and other EBV+ T- and NK-cell LPDs (n = 5). The ENKTCL cases highlighted some unusual features like indolent behavior, small cell morphology, and T-cell phenotype, including cases with CD4 and CD30 expression. The differential diagnosis of ENKTCL was illustrated by 4 cases with other primary cutaneous lymphomas. The difficulty in the diagnosis of systemic chronic active EBV disease, its complications, and the sometimes elusive boundaries among the EBV+ LPDs in children are also discussed. The submitted cases also unveiled cases of EBV+ γδ T-cell leukemia/lymphoma not recognized under current classifications and cases of EBV+ CD8+ cytotoxic lymphomas associated with treatment for B-cell lymphomas. The need to have a low threshold to investigate the presence of EBV is highlighted.

CONCLUSIONS

The diagnosis of EBV+ T- and NK-cell LPDs is complex and requires a multiparameter approach incorporating clinical information and morphologic and molecular features.

摘要

目的

总结2023年血液病理学学会/欧洲血液病理学协会研讨会关于爱泼斯坦-巴尔病毒(EBV)阳性T细胞和自然杀伤(NK)细胞淋巴增殖性疾病(LPD)的结论。

方法

38例病例提交至研讨会的第3场会议。

结果

病例包括结外NK/T细胞淋巴瘤(ENKTCL),鼻型(n = 16),儿童EBV阳性T细胞和NK细胞LPD(n = 12),原发性淋巴结EBV阳性T细胞和NK细胞淋巴瘤(n = 5),以及其他EBV阳性T细胞和NK细胞LPD(n = 5)。ENKTCL病例突出了一些不寻常的特征,如惰性行为、小细胞形态和T细胞表型,包括表达CD4和CD30的病例。4例其他原发性皮肤淋巴瘤病例说明了ENKTCL的鉴别诊断。还讨论了系统性慢性活动性EBV疾病的诊断困难、其并发症以及儿童EBV阳性LPD之间有时难以捉摸的界限。提交的病例还揭示了当前分类未识别的EBV阳性γδ T细胞白血病/淋巴瘤病例以及与B细胞淋巴瘤治疗相关的EBV阳性CD8 + 细胞毒性淋巴瘤病例。强调了对EBV存在进行调查的低阈值必要性。

结论

EBV阳性T细胞和NK细胞LPD的诊断复杂,需要采用结合临床信息以及形态学和分子特征的多参数方法。

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